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在“Elsevier电子期刊”中，命中：128条，耗时：小于0.01 秒

在所有数据库中总计命中：112条

1.From nocturnal frontal lobe epilepsy to Sleep-Related Hypermotor Epilepsy: A 35-year diagnostic challenge

作者：Paolo Tinuper^a ; ^b ; ^{paolo.tinuper@unibo.it} ; Francesca Bisulli^a ; ^b

关键词：Epilepsy ; Parasomnias ; Seizures during sleep ; Nocturnal frontal lobe epilepsy ; SHE ; Video-polysomnography

刊名：Seizure

出版年：2017

2.Effect of Intrathecal Baclofen on Delayed-Onset Paroxysmal Dystonia due to Compression Injury Resulting From Congenital and Progressive Spinal Bone Deformities in Chondrodysplasia Punctata

作者：Tetsuya Okazaki ; MD^a ; ^{t-okazaki@med.tottori-u.ac.jp" class="auth_mail" title="E-mail the corresponding author} ; Yoshiaki Saito ; MD ; PhD^a ; Riyo Ueda ; MD^a ; Susumu Sugihara ; MD^a ; Akiko Tamasaki ; MD ; PhD^a ; Yoko Nishimura ; MD^a ; Koyo Ohno ; MD^a ; Masami Togawa ; MD^a ; ^b ; Takako Ohno ; MD ; PhD^c ; Akiyoshi Horie ; MD ; PhD^d ; Masashi Honda ; MD ; PhD^e ; Atsushi Takenaka ; MD ; PhD^e ; Hideki Nagashima ; MD ; PhD^f ; Yoshihiro Maegaki ; MD ; PhD^a

关键词：brachytelephalangy ; spinal cord ; myelopathy ; atlantoaxial dislocation ; paroxysmal dystonia ; chondrodysplasia punctata ; detrusor-sphincter dyssynergia ; intrathecal baclofen

刊名：Pediatric Neurology

出版年：2016

3.Successful Treatment of Paroxysmal Movement Disorders of Infancy With Dimenhydrinate and Diphenhydramine

作者：Katherine M. Sawicka^a ; Helly Goez ; MD^b ; Richard J. Huntsman ; MD ; FRCP(C) ; CSCN(EEG)^c ; ^{dr.huntsman@usask.ca" class="auth_mail" title="E-mail the corresponding author}

关键词：benign paroxysmal tonic upward gaze of infancy ; transient paroxysmal dystonia of infancy ; dimenhydrinate ; diphenhydramine

刊名：Pediatric Neurology

出版年：2016

4.Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients

作者：Costanza Lamperti^a ; Federica Invernizzi^a ; Roberta Solazzi^b ; Elena Freri^b ; Francesco Carella^c ; Massimo Zeviani^d ; Federica Zibordi^b ; Carlo Fusco^e ; Giovanna Zorzi^b ; Tiziana Granata^b ; Barbara Garavaglia^a ; Nardo Nardocci^b ; ^{nnardocci@istituto-besta.it" class="auth_mail" title="E-mail the corresponding author}

关键词：PRRT2 ; Paroxysmal kinesigenic dyskinesia ; Epilepsy ; Dystonia ; Autosomal dominant

刊名：European Journal of Paediatric Neurology

出版年：2016

5.The α2β3γ2 GABA_A receptor preferring agonist NS11394 aggravates dystonia in the phenotypic dt^sz model

作者：Christine Sprö ; te ; Franziska Richter ; Anne Bauer ; Julia Gerstenberger ; Angelika Richter ; ^{angelika.richter@vetmed.uni-leipzig.de" class="auth_mail" title="E-mail the corresponding author}

关键词：GABA ; gamma-aminobutyric acid ; GABAA receptor ; gamma-aminobutyric acid type A receptor

刊名：European Journal of Pharmacology

出版年：2016

6.The Genetic Homogeneity of CAPOS Syndrome: Four New Patients With the c.2452G>A (p.Glu818Lys) Mutation in the ATP1A3 Gene

作者：Roderick P.P.W.M. Maas ; MD^a ; ^{roderick.maas@radboudumc.nl" class="auth_mail" title="E-mail the corresponding author} ; Jolanda H. Schieving ; MD^b ; Meyke Schouten ; MD^c ; Erik-Jan Kamsteeg ; PhD^c ; Bart P.C. van de Warrenburg ; MD ; PhD^a

关键词：CAPOS syndrome ; ATP1A3 gene ; cerebellar ataxia ; areflexia ; pes cavus ; optic atrophy ; sensorineural hearing loss

刊名：Pediatric Neurology

出版年：2016

7.Genetics in dystonia

作者：Christine Klein

关键词：Dystonia ; Genetics ; Classification ; Next generation sequencing ; Phenotype

刊名：Parkinsonism and Related Disorders

出版年：January, 2014

8.Psychogenic paroxysmal movement disorders - Clinical features and聽diagnostic clues

作者：Christos Ganos ; Maria Aguirregomozcorta ; Amit Batla ; Maria Stamelou ; Petra Schwingenschuh ; Alex ; er M眉nchau ; Mark J. Edwards ; Kailash P. Bhatia

关键词：Paroxysmal dyskinesias ; Psychogenic movement disorders ; PKD ; PNKD ; PED

刊名：Parkinsonism and Related Disorders

出版年：January, 2014

9.P93 - 2953: Identification of a new mutation of the SCL1A gene in a patient with GLUT1-DS

作者：T. Foiadelli ; M.V. Spartà ; N. Zavras ; C. Passera ; C. Gagliardone ; B. Rinaldi ; S. Valaperta ; F. Madia ; P. Veggiotti ; P. Striano ; S. Savasta

刊名：European Journal of Paediatric Neurology

出版年：2015

10.A novel ATP1A3 mutation with unique clinical presentation

作者：Hendrik Rosewich^a ; ¹ ; ^{hendrik.rosewich@med.uni-goettingen.de" class="auth_mail} ; Martina Baethmann^b ; ¹ ; ^{M.Baethmann@dritter-orden.de" class="auth_mail} ; Andreas Ohlenbusch^a ; ^{aohlenb@gwdg.de" class="auth_mail} ; Jutta Gä ; rtner^a ; ^{gaertnj@med.uni-goettingen.de" class="auth_mail} ; Knut Brockmann^c ; ^{kbrock@med.uni-goettingen.de" class="auth_mail}

关键词：Rapid-onset dystonia-parkinsonism ; Alternating hemiplegia of childhood ; ATP1A3 ; Paroxysmal flaccidity ; Eye closure ; Episodic weakness

刊名：Journal of the Neurological Sciences

出版年：15 June 2014

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